Evidence map›Paper›PMID 15630598›Full record

ArticleDer Nervenarzt2005

[Hereditary hemorrhagic telangiectasia. A rare treatable cause of stroke].

D Ecker, U W Geisthoff, M Juchems, G Schneider, A C Ludolph, J Kassubek, R Huber

Abstract readCase ReportsEnglish Abstract
PubMed Publisher
In one paragraph

Article in Der Nervenarzt, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.1field-weighted citation impact, top 39% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 1 country.

D EckerNeurologische Klinik und Poliklinik der Universität Ulm.
U W Geisthoff
M Juchems
G Schneider
A C Ludolph
J Kassubek
R Huber
Universität Ulm · DEKlinik und Poliklinik für Hals-Nasen-Ohren-Heilkunde · DEKlinik und Poliklinik für Neurologie · DEUniversitätsklinikum des Saarlandes · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease of the vascular connective tissue. Pulmonary arteriovenous and cerebral vascular malformations are risk factors for serious neurological complications such as paradoxical embolism and intracranial hematomas. We describe two patients with HHT and pulmonary arteriovenous malformations suffering from stroke caused by paradoxical embolism. In both cases, fistulas were successfully treated by embolisation and no further cerebral ischemic events occurred. In ischemic strokes of unknown origin, HHT should be considered as a possible diagnosis with effective treatment options.

Indexed as

AdultEmbolization, TherapeuticFemaleHumansMiddle AgedRare DiseasesStrokeTelangiectasia, Hereditary HemorrhagicTreatment Outcome

Identifiers

PMID15630598
OpenAlexW2911368654

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.